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Icotinib With Concurrent Radiotherapy vs Radiotherapy Alone in Older Adults With Unresectable Esophageal Squamous Cell Carcinoma: A Phase II Randomized Clinical Trial.
Luo, Honglei; Jiang, Wei; Ma, Li; Chen, Peng; Fang, Min; Ding, Lingyu; Hua, Yuhui; Du, Dexi; Jing, Zhao; Xie, Ruifei; Song, Yaqi; Wang, Jiayang; Zhou, Rongjing; Tian, Zhifeng; Wu, Shixiu.
Afiliação
  • Luo H; Department of Radiation Oncology, the Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
  • Jiang W; Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
  • Ma L; Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
  • Chen P; Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
  • Fang M; Department of Radiation Oncology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang, China.
  • Ding L; Department of Medical Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
  • Hua Y; Department of Pharmacy, Hangzhou Cancer Hospital, Hangzhou, China.
  • Du D; Department of Radiation Oncology, Lishui Central Hospital, Lishui, China.
  • Jing Z; Department of Radiation Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
  • Xie R; Department of Bio-informatics, Hangzhou Cancer Hospital, Hangzhou, China.
  • Song Y; Department of Radiation Oncology, the Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
  • Wang J; Department of Radiation Oncology, the Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
  • Zhou R; Department of Pathology, Hangzhou Cancer Hospital, Hangzhou, China.
  • Tian Z; Department of Radiation Oncology, Lishui Central Hospital, Lishui, China.
  • Wu S; Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
JAMA Netw Open ; 3(10): e2019440, 2020 10 01.
Article em En | MEDLINE | ID: mdl-33026449
ABSTRACT
Importance Palliative radiotherapy (RT) is generally recommended for older patients with esophageal squamous cell carcinoma (ESCC) with poor prognosis. A new combination treatment is therefore needed.

Objective:

To assess the efficacy and toxicity of RT plus icotinib vs RT alone in older patients with ESCC. Design, Setting, and

Participants:

This randomized, multicenter, open-label, phase II clinical trial was conducted in China, with enrollment between January 1, 2015, and October 31, 2016. Patients aged 70 years or older with clinical stage T2 to T4, N0/1, M0/1a unresectable (because of comorbidities, T4 disease, unresectable lymph node, or refused surgery) ESCC were randomized 11 to receive RT plus icotinib or RT alone. Radiation was prescribed at 60 Gy in 30 fractions in both groups, and icotinib was administered at a dosage of 125 mg 3 times a day in the RT plus icotinib group. The last follow-up was completed on June 30, 2019, and data were analyzed from July 1 to September 30, 2019.

Interventions:

Patients were randomized to either RT plus icotinib or RT alone. Main Outcomes and

Measures:

The primary end point was overall survival (OS). Treatment-related toxic effects were evaluated. Immunohistochemistry was performed to analyze epidermal growth factor receptor (EGFR) expression if available.

Results:

A total of 127 patients (median age, 76 years [range, 70-91 years]; 76 men [59.8%]) were enrolled and were eligible for survival analysis. Median OS was 24.0 (95% CI, 22.2-25.8) months in the RT plus icotinib group vs 16.3 (95% CI, 13.8-18.8) months in the RT group (hazard ratio, 0.53; 95% CI, 0.33-0.87; P = .008). No difference was observed in grades 3 or 4 adverse events. Patients with EGFR overexpression had a significantly better median overall survival (not reached vs 16.3 months [range, 2.6-45.1 months]; P = .03) in the RT plus icotinib group. Conclusions and Relevance In this randomized clinical trial, icotinib plus RT was well tolerated and improved OS in older patients with ESCC relative to RT alone. Patients with EGFR overexpression benefitted more from icotinib with RT. Trial Registration ClinicalTrials.gov Identifier NCT02375581.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinazolinas / Neoplasias Esofágicas / Éteres de Coroa / Quimiorradioterapia / Carcinoma de Células Escamosas do Esôfago / Antineoplásicos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: JAMA Netw Open Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinazolinas / Neoplasias Esofágicas / Éteres de Coroa / Quimiorradioterapia / Carcinoma de Células Escamosas do Esôfago / Antineoplásicos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Revista: JAMA Netw Open Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China
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